CLASS II ONGOING Device recall · Reported 1 Oct 2025 · FDA Enforcement Report
Juggerknot Mini Soft Anchors recalled by Biomet
Biomet is recalling Juggerknot Mini Soft Anchors, distributed nationwide in the US. The recall was initiated on 9 Sep 2025 and the FDA has classified it as Class II.
Check your package
Stop using the device if the notice says to, and contact the manufacturer or your healthcare provider for the correction or replacement.
Recall details
- Recall number
- Z-2619-2025
- FDA event ID
- 97570
- Recalling firm
- Biomet, Warsaw, IN
- Classification
- Class II
- Status
- Ongoing
- Recall initiated
- 9 Sep 2025
- FDA classified
- 23 Sep 2025
- Reported
- 1 Oct 2025
- Type
- Voluntary: Firm initiated
- Customers notified by
- Letter
- Reason category
- Other Reasons
- Device type
- Other Medical Devices
Timeline
| 9 Sep 2025 | Recall initiated by company | |
| 23 Sep 2025 | Classified by FDA | +14 days |
| 1 Oct 2025 | Published in enforcement report | +8 days |
Companies usually start a recall weeks before the FDA classifies and publishes it; the gap above is that lag.
Reason for recall
The outer carton box label is for the JuggerKnot 1.0mm Mini products. However, the products within the carton are JuggerKnot 1.4mm Short devices.
Product as listed by the FDA
Juggerknot Mini Soft Anchors, Model/Catalog Number: 912080
Where it was distributed
US Nationwide distribution.
Questions about this recall
Why was it recalled?
The outer carton box label is for the JuggerKnot 1.0mm Mini products. However, the products within the carton are JuggerKnot 1.4mm Short devices.
Which lots are affected?
UDI-DI: 00880304520950; Lot Number 0002713620
Where was it sold?
US Nationwide distribution.
What should I do if I have it?
Stop using the device if the notice says to, and contact the manufacturer or your healthcare provider for the correction or replacement.
What does Class II mean?
Class II means the product may cause temporary or medically reversible health problems, or the probability of serious harm is remote.
Read the official FDA notice · Source record retrieved 26 Sep 2026. The FDA describes openFDA data as unvalidated; the official notice takes precedence. This page reports the record and gives no medical advice.
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